This research demonstrates selective glycerol oxidation to glyceric acid using mixed-metal oxide catalysts, indicating potential for sustainable biomass valorization.
Thermal valorization of surplus biomass-derived feedstocks such as glycerol into high-value chemicals represents a sustainable strategy for biomass utilization and decarbonization of chemical manufacturing. However, conventional glycerol conversion processes are often restricted to low-value C1 products owing to rapid C–C bond cleavage during thermo-oxidation. Herein, we report highly efficient Au-Pt bimetallic alloy catalysts supported on mixed-oxide catalysts that enable the selective oxidation of glycerol under ambient conditions in the absence of a base. The synergistic interaction between Au and Pt promotes preferential oxidation of the terminal hydroxyl groups while preserving the C3 backbone, thereby affording the desirable C3 product, glyceric acid. The single-factor experiments and response surface analysis demonstrated that the Au-Pt bimetallic alloy catalysts supported on the mixed oxide MgO-Al2O3 exhibited a glycerol conversion of up to 82.0% and a glyceric acid selectivity of 62.1% under favorable reaction conditions. Kinetic studies further indicated that the activation energy of this catalyst in the reaction system is 32.7 kJ/mol.
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Wang et al. (2025) studied this question.
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